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In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery
INTRODUCTION: As a topical delivery system, a nanoscaled emulsion is considered a good carrier of several active ingredients that convey several side effects upon oral administration, such as nonsteroidal anti-inflammatory drugs (NSAIDs). OBJECTIVE: We investigated the in vitro permeation properties...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3075904/ https://www.ncbi.nlm.nih.gov/pubmed/21499428 http://dx.doi.org/10.2147/IJN.S14667 |
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author | Abdullah, Ghassan Z Abdulkarim, Muthanna F Salman, Ibrahim M Ameer, Omar Z Yam, Mun F Mutee, Ahmed F Chitneni, Mallikarjun Mahdi, Elrashid S Basri, Mahiran Sattar, Munavvar A Noor, Azmin M |
author_facet | Abdullah, Ghassan Z Abdulkarim, Muthanna F Salman, Ibrahim M Ameer, Omar Z Yam, Mun F Mutee, Ahmed F Chitneni, Mallikarjun Mahdi, Elrashid S Basri, Mahiran Sattar, Munavvar A Noor, Azmin M |
author_sort | Abdullah, Ghassan Z |
collection | PubMed |
description | INTRODUCTION: As a topical delivery system, a nanoscaled emulsion is considered a good carrier of several active ingredients that convey several side effects upon oral administration, such as nonsteroidal anti-inflammatory drugs (NSAIDs). OBJECTIVE: We investigated the in vitro permeation properties and the in vivo pharmacodynamic activities of different nanoscaled emulsions containing ibuprofen, an NSAID, as an active ingredient and newly synthesized palm olein esters (POEs) as the oil phase. METHODOLOGY: A ratio of 25:37:38 of oil phase:aqueous phase:surfactant was used, and different additives were used for the production of a range of nanoscaled emulsions. Carbopol(®) 940 dispersion neutralized by triethanolamine was employed as a rheology modifier. In some circumstances, menthol and limonene were employed at different concentrations as permeation promoters. All formulae were assessed in vitro using Franz diffusion cell fitted with full-thickness rat skin. This was followed by in vivo evaluation of the anti-inflammatory and analgesic activities of the promising formulae and comparison of the effects with that of the commercially available gel. RESULTS AND DISCUSSION: Among all other formulae, formula G40 (Carbopol(®) 940-free formula) had a superior ability in transferring ibuprofen topically compared with the reference. Carbopol(®) 940 significantly decreased the amount of drug transferred from formula G41 through the skin as a result of swelling, gel formation, and reduction in drug thermodynamic activity. Nonetheless, the addition of 10% w/w of menthol and limonene successfully overcame this drawback since, relative to the reference, higher amount of ibuprofen was transferred through the skin. By contrast, these results were relatively comparable to that of formula G40. Pharmacodynamically, the G40, G45, and G47 formulae exhibited the highest anti-inflammatory and analgesic effects compared with other formulae. CONCLUSION: The ingredients and the physical properties of the nanoscaled emulsions produced by using the newly synthesized POEs succeeded to deliver ibuprofen competently. |
format | Text |
id | pubmed-3075904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30759042011-04-15 In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery Abdullah, Ghassan Z Abdulkarim, Muthanna F Salman, Ibrahim M Ameer, Omar Z Yam, Mun F Mutee, Ahmed F Chitneni, Mallikarjun Mahdi, Elrashid S Basri, Mahiran Sattar, Munavvar A Noor, Azmin M Int J Nanomedicine Original Research INTRODUCTION: As a topical delivery system, a nanoscaled emulsion is considered a good carrier of several active ingredients that convey several side effects upon oral administration, such as nonsteroidal anti-inflammatory drugs (NSAIDs). OBJECTIVE: We investigated the in vitro permeation properties and the in vivo pharmacodynamic activities of different nanoscaled emulsions containing ibuprofen, an NSAID, as an active ingredient and newly synthesized palm olein esters (POEs) as the oil phase. METHODOLOGY: A ratio of 25:37:38 of oil phase:aqueous phase:surfactant was used, and different additives were used for the production of a range of nanoscaled emulsions. Carbopol(®) 940 dispersion neutralized by triethanolamine was employed as a rheology modifier. In some circumstances, menthol and limonene were employed at different concentrations as permeation promoters. All formulae were assessed in vitro using Franz diffusion cell fitted with full-thickness rat skin. This was followed by in vivo evaluation of the anti-inflammatory and analgesic activities of the promising formulae and comparison of the effects with that of the commercially available gel. RESULTS AND DISCUSSION: Among all other formulae, formula G40 (Carbopol(®) 940-free formula) had a superior ability in transferring ibuprofen topically compared with the reference. Carbopol(®) 940 significantly decreased the amount of drug transferred from formula G41 through the skin as a result of swelling, gel formation, and reduction in drug thermodynamic activity. Nonetheless, the addition of 10% w/w of menthol and limonene successfully overcame this drawback since, relative to the reference, higher amount of ibuprofen was transferred through the skin. By contrast, these results were relatively comparable to that of formula G40. Pharmacodynamically, the G40, G45, and G47 formulae exhibited the highest anti-inflammatory and analgesic effects compared with other formulae. CONCLUSION: The ingredients and the physical properties of the nanoscaled emulsions produced by using the newly synthesized POEs succeeded to deliver ibuprofen competently. Dove Medical Press 2011 2011-02-17 /pmc/articles/PMC3075904/ /pubmed/21499428 http://dx.doi.org/10.2147/IJN.S14667 Text en © 2011 Abdullah et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Abdullah, Ghassan Z Abdulkarim, Muthanna F Salman, Ibrahim M Ameer, Omar Z Yam, Mun F Mutee, Ahmed F Chitneni, Mallikarjun Mahdi, Elrashid S Basri, Mahiran Sattar, Munavvar A Noor, Azmin M In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery |
title | In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery |
title_full | In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery |
title_fullStr | In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery |
title_full_unstemmed | In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery |
title_short | In vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery |
title_sort | in vitro permeation and in vivo anti-inflammatory and analgesic properties of nanoscaled emulsions containing ibuprofen for topical delivery |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3075904/ https://www.ncbi.nlm.nih.gov/pubmed/21499428 http://dx.doi.org/10.2147/IJN.S14667 |
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